Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer (Q39995775)

16 September 2017

Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer (English)

1 reference

16 September 2017

Holmberg E

1

1 reference

16 September 2017

Rozell BL

series ordinal

2

1 reference

16 September 2017

Toftgård R

series ordinal

3

1 reference

16 September 2017

language of work or name

English

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publication date

1 July 1996

1 reference

British Journal of Cancer

16 September 2017

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16 September 2017

74

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16 September 2017

2

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16 September 2017

246-250

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https://scigraph.springernature.com/pub.10.1038/bjc.1996.345

16 September 2017

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cites work

Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers.

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Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.

22 September 2017

1 reference

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Complications of the naevoid basal cell carcinoma syndrome: results of a population based study

22 September 2017

1 reference

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Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Localization of the gene for the nevoid basal cell carcinoma syndrome.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

The 1993-94 Généthon human genetic linkage map

22 September 2017

1 reference

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Nevoid basal-cell carcinoma syndrome

22 September 2017

1 reference

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Biology of basal cell carcinoma (Part I).

22 September 2017

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A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma

22 September 2017

1 reference

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Biology of cutaneous squamous cell carcinoma

22 September 2017

1 reference

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Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

22 September 2017

1 reference

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Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology

22 September 2017

1 reference

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Progression of basal cell carcinoma through loss of chromosome 9q and inactivation of a single p53 allele.

15 June 2018

1 reference

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Analysis of p53 gene mutations and loss of heterozygosity for loci on chromosome 9q in basal cell carcinoma

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Basal cell carcinomas and squamous cell carcinomas of human skin show distinct patterns of chromosome loss.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Genetic instability of microsatellite markers in region q22.3-q31 of chromosome 9 in skin squamous cell carcinomas

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Accumulation of genetic alterations during esophageal carcinogenesis.

15 June 2018

1 reference

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Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

15 June 2018

1 reference

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Microsatellite instability in human non-melanoma and melanoma skin cancer

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Sunlight exposure, pigmentary factors, and risk of nonmelanocytic skin cancer. I. Basal cell carcinoma

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Delineation of two distinct deleted regions on chromosome 9 in human non-melanoma skin cancers

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Detailed deletion mapping of chromosome 9q in bladder cancer: evidence for two tumour suppressor loci

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Localisation of gene for the naevoid basal-cell carcinoma syndrome

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Location of gene for Gorlin syndrome

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

The emerging epidemic of skin cancer

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Low incidence of Ha-ras oncogene mutations in human epidermal tumors

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074566

Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry

20 August 2018

1 reference

12 December 2020

An allelotype of squamous carcinoma of the head and neck using microsatellite markers

1 reference

12 December 2020

High frequency of loss of heterozygosity in actinic keratoses, a usually benign disease

1 reference

12 December 2020

Extraction of high quality genomic DNA from microsamples of human blood

1 reference

12 December 2020

Sunlight exposure, pigmentation factors, and risk of nonmelanocytic skin cancer. II. Squamous cell carcinoma

1 reference

12 December 2020

Deletion mapping in squamous cell carcinomas of the esophagus defines a region containing a tumor suppressor gene within a 4-centimorgan interval of the distal long arm of chromosome 9

1 reference

12 December 2020

Identifiers

DOI

10.1038/BJC.1996.345

1 reference

release_qhkz7ty6hfejdgepcgknrzodru

16 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qhkz7ty6hfejdgepcgknrzodru

24 November 2022

mapped directly with Wikidata item

1 reference

16 September 2017

PubMed publication ID

8688329

1 reference